Skip to main content
. 2019 Oct 16;7(10):462. doi: 10.3390/microorganisms7100462

Table 2.

Details of the primers used for PCR amplification of EscN/YscN/HrcN family type III secretion system ATPase (hrcN), chromosomal replication initiator factor (dnaA), DNA topoisomerase (ATP-hydrolyzing) subunit B (gyrB), type I glyceraldehyde-3-phosphate dehydrogenase (gapA), hydroxymethylbilane synthase (hmbs), and pyruvate dehydrogenase (pdg) gene.

Target Gene Primers Name Primer Sequences (5′-3′) Product Size
hrcN X-hrcN-F TCGGCACCATGCTCAAGGT 846
X-hrcN-F GTGTAGAACGCGGTGATCGA
dnaA dnaA-F CAGCACGGTGGTGTGGTC 928
dnaA-R CCTGGATTCGCATTACACC
gyrB GyrB-F2 GAGGTGATCCTCACCGTGCT 841
GyrB-R2 TGATGGCCTTGGCTTCGTTC
gapA gapA-F1 TGGCCATCAATGACCTGCTC 865
gapA-R1 TAGCCCCACTCGTTGTCGTA
pdg pdg-F CCACCCACCAGACCAAGAA 990
pdg-R CAGGTACATGCCCTTGATGA
hmbs Hmbs-F GTATCGCCACCCGCAAAA 873
Hmbs-R CCTTGTCGAACAGCCCTTG
Hmbs-F2 TTGCATCGCCACCCGCAAGA 837
Hmbs-R2 TCCTTGTCGAACAGGCCTTG
Hmbs-F10 AGGGCCTGTTTTTGAAGGAA 595
Hmbs-R10 AACCCCTCGCCTTCCCAGGT